Dimethyl Sulfoxide → 3-methyl-1-{3-(phenyl)propyl}-1H-indole-6-carboxaldehyde

HRID 392217Notes

Reaction equation

HRID 392217 reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH3:11][C:12]1[C:20]2[C:15](=[CH:16][C:17]([CH2:21][OH:22])=[CH:18][CH:19]=2)[N:14]([CH2:23][CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:13]=1.C(N(CC)CC)C>ClCCl.O>[CH3:11][C:12]1[C:20]2[C:15](=[CH:16][C:17]([CH:21]=[O:22])=[CH:18][CH:19]=2)[N:14]([CH2:23][CH2:24][CH2:25][C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH:13]=1

Participants

7

Procedure

Dimethylsulphoxide (0.311 g) was added to a stirring solution of oxalyl chloride in dichloromethane (1 ml, 2M) in dichloromethane (25 ml) at −60° C. under argon and the mixture was stirred for 2 minutes. A solution of 3-methyl-1-{3-(phenyl)propyl}-1H-indole-6-methanol [0.501 g, Reference Example 22(c)] in dichloromethane (10 ml) was then added dropwise and the mixture stirred for 15 minutes at −60° C. Triethylamine (0.956 g) was then added and the solution warmed to room temperature and stirred for 1 hour. The mixture was poured into water (20 ml) and then extracted three times with dichloromethane (25 ml). The combined extracts were washed with brine (30 ml), then dried over sodium sulphate and then evaporated. The residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and hexane (1:1, v/v) to yield the title compound (0.283 g).

Workup

  1. stirringthe mixture stirred for 15 minutes at −60° C
  2. stirringstirred for 1 hour
  3. extractionextracted three times with dichloromethane (25 ml)
  4. washThe combined extracts were washed with brine (30 ml)
  5. dry with materialdried over sodium sulphate
  6. customevaporated
  7. additionThe residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and hexane (1:1

Sources & evidence

ORD record
ord-f4e89fccef5f40b494ab98ed52c10c83
Source dataset
uspto-grants-2004_10
Patent number
US06800645B1

Reaction notes

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